“Meet Max” – Mikelle Meet Max. Six years ago (almost seven), my life changed when he was born. He was my first child and the most amazing gift to me […]
“Meet Max” – Mikelle Meet Max. Six years ago (almost seven), my life changed when he was born. He was my first child and the most amazing gift to me […]
“Those Who ‘Get It’” – Janet My 7 year old son has CTD and Autism. He was diagnosed with CTD January 2012 and then Autism, September that same year. At […]
“Seasons” – Nathan Well friends, the end of summer is again upon us. Children are heading back to school and hopefully, soon the cool air of fall will again give […]
“Oops, Sorry!” – Jess Today I am writing about one of William’s favourite phrases – “Oops, sorry!”. He is 5 and has Creatine Transporter Deficiency (CTD).
GAMT Newborn Screening Update – Kim In May, the ACD met with the Advisory Committee on Heritable Disorders in Newborns and Children (ACHDNC). GAMT was nominated for inclusion on the […]
“A Mother’s Intuition and How One Family Never Gave Up” – Whitnie Parents have a sixth sense about their children. Call it a hunch, a gut feeling or a Mother’s/Father’s […]
“The Parker Family” – Melissa “There have been angels in my life….” This was written to me on a thank you note by the wife of a friend who passed […]